Modular Electromechanical Surgical System
Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.
OpenFDA device adverse-event casebook.
FDA Class II (moderate risk, special controls required), regulated under 21 CFR §878.4964 (General, Plastic Surgery panel).
FDA MAUDE casebook
openFDA event book Modular Electromechanical Surgical System LIGHT-BOOK · MAUDE
#559 of 1000 · 1,552 reports · 2025–2026
- BOOK 1,552 reports
- RANK #559 of 1000
- DEATH 0 death-typed
- INJ 31 injury-typed
- MALF 1,521 malfunction
- SPAN 2025–2026
- PEAK 2026: 1,468
- PHOTO Reagent
Nearest event-volume peer: Reagent, Coronavirus Serological (2 report gap)
Modular Electromechanical Surgical System sits #559 of 1000 among tracked device types with 1,552 MAUDE reports spanning 2025–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →
Malfunction reports run above the device-type norm
Modular Electromechanical Surgical System carries 98.0% MALFUNCTION-coded reports, 33.2pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
- INJ 2.0% corpus 30.3% · below corpus mean (-28.3 pp)
- MALF 98.0% corpus 64.8% · above corpus mean (+33.2 pp)
Lead product-problem code Communication or Transmission Problem is 14% of coded problems · Lead manufacturer COVIDIEN SURGICAL accounts for 83% of manufacturer-tagged reports · Top event location is 100% of location-tagged rows .
Modular Electromechanical Surgical System in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Device
Device, Removal, Pacemaker Electrode, Percutaneous
1,561 reports
- Barrier
Barrier, Absorbable, Adhesion
1,558 reports
- Modular Elect… (this)
Modular Electromechanical Surgical System
1,552 reports
- Reagent
Reagent, Coronavirus Serological
1,550 reports
- Catheter
Catheter, Umbilical Artery
1,545 reports
- Toothbrush
Toothbrush, Manual
1,544 reports
What this shows Modular Electromechanical Surgical System carries 1,552 MAUDE reports, ranked #559 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Related Entities for Modular Electromechanical Surgical System
Top Manufacturers
Event Locations
Nationwide devices with a comparable report-volume footprint
Modular Electromechanical Surgical System carries zero death-typed MAUDE reports, so the peer set below compares report volume only; both axes are floored at ≥100 reports so the neighborhood stays in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (1,552 here).
Similar death-typed counts
Nearest other device types by death-typed report count (0 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Modular Electromechanical Surgical System are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.
Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Modular Electromechanical Surgical System; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.